Package 60760-743-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 60760-743-90
Digits Only 6076074390
Product NDC 60760-743
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-743-90)

Marketing

Marketing Status
Marketed Since 2021-01-28
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bd575b8-2980-75d8-e063-6394a90a8d2a", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["ba4d863d-be38-8cf5-e053-2995a90a69fb"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-743-90)", "package_ndc": "60760-743-90", "marketing_start_date": "20210128"}], "brand_name": "Gabapentin", "product_id": "60760-743_4bd575b8-2980-75d8-e063-6394a90a8d2a", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60760-743", "generic_name": "Gabapentin", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20210128", "listing_expiration_date": "20271231"}